Human Catn C ELISA Kit

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  • Alternative name

    Dipeptidyl peptidase 1 ELISA KIT; Cathepsin C ELISA KIT; Cathepsin J ELISA KIT; Dipeptidyl peptidase I ELISA KIT; DPP-I ELISA KIT; DPPI ELISA KIT; Dipeptidyl transferaseCleaved into the following 3 chains:Dipeptidyl peptidase 1 exclusion domain chainAlternative name(s):Dipeptidyl peptidase I exclusion domain chainCTSC ELISA KIT; CPPI ELISA KIT; DPP-I ELISA KIT; DPPI ELISA KIT

  • Catalog
    E007015
  • species
    Human
  • GeneCatn C
  • Standard CurveHuman Catn C ELISA Kit
  • Other Species Mouse Catn-C ELISA Kit
  • SamplesSerum, Plasma , tissue homogenates,Cell culture supernates,Other biological fluids.
  • Sensitivity0.1 ng/mL.
  • Intended UseHuman Catn C ELISA Kit allows for the in vitro quantitative determination of Catn C , concentrations in serum, Plasma , tissue homogenates and Cell culture supernates and Other biological fluids.
  • StorageFor 5-7days:Store the whole kit at 4℃
    For a Long time :Store the Substrate at 4℃, other reagent should store at -20℃.
  • Product Description
    specifical
    Principle of the Assay: Catn-C ELISA kit applies the quantitative sandwich enzyme immunoassay technique. The microtiter plate has been pre-coated with a monoclonal antibody specific for Catn-C. Standards or samples are then added to the microtiter plate wells and Catn-C if present, will bind to the antibody pre-coated wells. In order to quantitatively determine the amount of Catn-C present in the sample, a standardized preparation of horseradish peroxidase (HRP) -conjugated polyclonal antibody, specific for Catn-C are added to each well to "sandwich" the Catn-C immobilized on the plate. The microtiter plate undergoes incubation, and then the wells are thoroughly washed to remove all unbound components. Next, substrate solutions are added to each well. The enzyme (HRP) and substrate are allowed to react over a short incubation period. Only those wells that contain Catn-C and enzyme-conjugated antibody will exhibit a change in color. The enzyme-substrate reaction is terminated by addition of a sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450 nm. A standard curve is plotted relating the intensity of the color (O.D.) to the concentration of standards. The Catn-C concentration in each sample is interpolated from this standard curve.


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